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Blood Advances|February 4, 2026
Impact of Iron Overload on Hematopoietic Stem Cell Transplant in Children with Non-Malignant Hematological DisordersNora M Gibson, Nhat Thi Duy Nguyen, Sandra Amaral, et al.
Frontiers in Physiology|July 24, 2019
The Spectrum of SPTA1-Associated Hereditary SpherocytosisSatheesh Chonat, Mary Risinger, Haripriya Sakthivel, et al.
Frontiers in Physiology|November 19, 2019
Corrigendum: The Spectrum of SPTA1-Associated Hereditary SpherocytosisSatheesh Chonat, Mary Risinger, Haripriya Sakthivel, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 29, 2008
Bone disease in thalassemia: a frequent and still unresolved problemMaria G Vogiatzi, Eric A Macklin, Ellen B Fung, et al.
Blood Advances|August 26, 2022
Deferiprone for transfusional iron overload in sickle cell disease and other anemias: open-label study of up to 3 yearsMohsen S Elalfy, Mona Hamdy, Amal El-Beshlawy, et al.
FEMS Microbiology Ecology|June 14, 2022
Investigation of active site amino acid influence on carbon and chlorine isotope fractionation during reductive dechlorinationElizabeth Phillips, Olivia Bulka, Katherine Picott, et al.
Transfusion|May 18, 2021
Screening for new red blood cell alloantibodies after transfusion in patients with sickle cell diseaseAlexander Rankin, Deepika Darbari, Andrew Campbell, et al.
British Journal of Haematology|May 29, 2020
The pyruvate kinase (PK) to hexokinase enzyme activity ratio and erythrocyte PK protein level in the diagnosis and phenotype of PK deficiencyHanny Al-Samkari, Kathryn Addonizio, Bertil Glader, et al.
Military Medicine|December 15, 2021
Characteristics of Active Duty Service Members Referred to the Navy's Weight-Management ProgramErin L Miggantz, Karla Materna, Matthew S Herbert, et al.
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